Crystalline Forms of (-)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride

ABSTRACT

A hitherto unknown crystalline form of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride, pharmaceutical compositions containing the new crystalline form, methods of producing the new crystalline form, and a related method of use including treatment of, e.g., pain and/or urinary incontinence.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of application Ser. No. 14/930,337, filed on Nov. 2, 2015, which is a continuation of application Ser. No. 14/304,313, filed on Jun. 13, 2014, which is a continuation of application Ser. No. 13/923,891, filed on Jun. 21, 2013, which is continuation of co-pending application Ser. No. 13/565,867, filed Aug. 3, 2012, which in turn was a continuation of application Ser. No. 13/172,009, filed Jun. 29, 2011, now abandoned, which in turn was a continuation of application Ser. No. 12/634,777, filed Dec. 10, 2009, now U.S. Pat. No. 7,994,364, issued on Aug. 9, 2011, which was a continuation of application Ser. No. 12/274,747, filed Nov. 20, 2008, now abandoned, which was a continuation of application Ser. No. 11/646,232, filed Dec. 28, 2006, now abandoned, which was a continuation of International patent application no. PCT/EP2005/006884, filed Jun. 27, 2005, which claims benefit of European patent application Serial No. 04015091.4 filed Jun. 28, 2004, the entire disclosures of each of which are hereby incorporated in their entirety.

FIELD OF THE INVENTION

This invention relates to solid crystalline forms of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride compounds, methods of producing these compounds, and related treatments, including use as analgesics as well as pharmaceutical compositions containing these compounds.

BACKGROUND OF THE INVENTION

The treatment of pain conditions is of great importance in medicine. There is currently a world-wide need for additional pain therapy. The pressing requirement for a target-oriented treatment of pain conditions which is right for the patient, which is to be understood as the successful and satisfactory treatment of pain for the patients, is documented in the large number of scientific works which have recently and over the years appeared in the field of applied analgesics or on basic research on nociception.

BRIEF SUMMARY OF THE INVENTION

One object of the present invention is to provide new solid forms of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride useful in the treatment or inhibition of pain.

U.S. Pat. Nos. 6,248,737 and 6,344,558 as well as European Patent EP 693 475 B1 disclose the substance and the synthesis of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride in example 25. As proven by X-ray diffraction the 1R,2R configuration as shown in the drawing of the structure in example 25 is correct although the configuration is reported as (−)-(1R,2S) in U.S. Pat. No. 6,248,737 and (−)-(1S,2S) in U.S. Pat. No. 6,344,558 as well as in EP 693 475 B1.

It has now been surprisingly found that (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride can be produced in a reproducible manner in two different crystalline forms. The present invention provides a new form (Form A) of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride which is different from the form already known (Form B) obtained by the procedure described in example 25 of U.S. Pat. No. 6,248,737 and U.S. Pat. No. 6,344,558 as well as EP 693 475 B1. This new Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride is very stable at ambient conditions and therefore useful for producing a pharmaceutical composition.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows an X-ray diffraction pattern;

FIG. 2 shows an infrared spectrum;

FIG. 3 shows a RAMAN spectrum;

FIG. 4 shows an X-ray diffraction pattern;

FIG. 5 shows an infrared spectrum;

FIG. 6 shows a RAMAN spectrum;

FIG. 7 shows an X-ray diffraction pattern;

FIG. 8 shows an X-ray diffraction pattern

SUMMARY OF THE INVENTION

The new crystalline Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride can be identified by X-ray powder diffraction. The X-ray diffraction (“XRPD”) pattern is shown in FIG. 1 with the peak listing shown as Table 1.

The most important X-ray lines (2-theta values) in terms of intensity characterizing Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride showing one or a combination of the following in a powder diffraction measurement when measured using Cu K_(α) radiation at ambient temperature are 14.5±0.2, 18.2±0.2, 20.4±0.2, 21.7±0.2 and 25.5±0.2.

To discriminate crystalline Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride from Form B it is more advantageous to look at the unique peaks in the X-ray diffraction diagram, i.e. e.g. the lines with sufficient intensity at 2-theta values, where Form B does not show lines with significant intensity. Such characteristic X-ray lines (2-theta values) for Form A in a powder diffraction pattern when measured using CuK_(α) radiation at ambient temperature are: 15.1±0.2, 16.0±0.2, 18.9±0.2, 20.4±0.2, 22.5±0.2, 27.3±0.2, 29.3±0.2 and 30.4±0.2.

Another method to identify crystalline Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride is IR-spectroscopy. The IR-Spectrum of Form A is shown as FIG. 2 with the peak listing shown in comparison to Form B as Table 2.

In the IR-spectrum it is characteristic for crystalline Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride to show a combination of the following IR bands: 3180±4 cm⁻¹, 2970±4 cm⁻¹, 2695±4 cm⁻¹, 2115±4 cm⁻¹, 1698±4 cm⁻¹, 1462±4 cm⁻¹, 1032±4 cm⁻¹ and/or 972±4 cm⁻¹.

RAMAN technique can also be used to identify of the crystalline Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride. Especially the range between 800 cm⁻¹ and 200 cm⁻¹, which is shown in FIG. 3, is advantageously used also by way of RAMAN microscopy.

Crystal structure analysis of Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride showed monoclinic crystals with the following parameters of the elemental cell (length of side and angle):

-   -   a: 7.11 Å     -   b: 11.62 Å     -   c: 17.43 Å     -   β: 95.0°.

The elemental cell of the crystal of crystalline Form A has a volume of 1434±5 Å³ and a calculated density of 1.20±0.01 g/cm³.

The invention further relates to processes for the preparation of crystalline Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride.

The process starts from crystalline Form B of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride prepared according to U.S. Pat. Nos. 6,248,737 or 6,344,558 or European Patent EP 693 475 B1 incorporated herein by reference.

In one embodiment of the process (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form A is produced by dissolving the (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form B in acetone, acetonitrile or isopropanol, optionally followed by filtering, leaving the solution to crystallize and isolating the crystals of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form A preferably by filtering again.

If acetone or acetonitrile is used it is preferred that during this process the temperature is kept below +40° C., more preferably below +25° C., especially after filtering. It is further preferred that in this process between 5 mg and 1 mg, more preferably between 2.5 mg and 1.4 mg, especially between 2.0 mg and 1.4 mg (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride is dissolved per ml solvent.

The use of isopropanol is preferred, if seed crystals of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form A are available. The isopropanol used preferably contains about 0.5% per volume of water. The dissolution of the (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form B in isopropanol is performed at temperatures above room temperature, preferably above 65° C. but not exceeding 80° C. After complete dissolution the heat is turned of and the seed crystals are added during a first cooling phase. Thereafter the resulting mixture is cooled down to ≦15° C., preferably ≦10° C. and especially ≦5° C.

Optionally it is possible to reduce the solvent by evaporation, preferably in an evaporator under reduced pressure. Preferably the remaining volume of the solution after evaporation should not be less than 20% of the volume at the beginning of the process. Optionally it is also possible to add active carbon to the solution originally prepared.

In a preferred embodiment of the invention the (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form A obtained by the process described above is redissolved in acetone acetonitrile or isopropanol, preferably in the solvent already used in the first step, optionally is filtered to remove any insoluble residue and, optionally after reducing the amount of solvent by evaporation, is left to crystallize.

It is preferred that in the last crystallization step the temperature is maintained at ≦15° C., more preferably ≦10° C. and especially ≦5° C.

In a further embodiment of the process according to the invention (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form A is produced in the solid state by cooling (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form B between 24 h and 168 h to a temperature between −4° C. and −80° C. It is preferred that in this process the cooling temperature is between −10° C. and −60° C., preferably between −15° C. and −50° C., especially between −25° C. and −40° C. and the cooling is carried out for a time between 24 h and 120 h, preferably between 24 h and 72 h, especially between 24 h and 48 h.

This invention further relates to a new Crystalline Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride obtainable by dissolving (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of Form B in acetonitrile together with active carbon, heating the solution to the boiling point, removing the active carbon by filtering, stirring the solution at a temperature below 40° C., removing insoluble residue by filtering and removing part of the solvent leaving (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of Form A to crystallize, redissolving the crystals so obtained in acetonitrile, removing insoluble residue by filtering and removing part of the solvent leaving (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of Form A to crystallize.

Crystalline Form A according to the invention has the same pharmacological activity as Form B but is more stable under ambient conditions. It can be advantageously used as active ingredient in pharmaceutical compositions.

Therefore the invention further relates to a pharmaceutical composition containing as active ingredient (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form A according to the invention and at least one suitable additive and/or auxiliary substance.

Such pharmaceutical composition according to the invention contains, in addition to crystalline Form A (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride, one or more suitable additive and/or auxiliary substance such as for example carrier materials, fillers, solvents, diluents, coloring agents and/or binders, and may be administered as liquid medicament preparations in the form of injectable solutions, drops or juices, as semi-solid medicament preparations in the form of granules, tablets, pellets, patches, capsules, plasters or aerosols. The choice of the auxiliary substances, etc., as well as the amounts thereof to be used depend on whether the medicament is to be administered orally, per orally, parenterally, intravenously, intraperitoneally, intradermally, intramuscularly, intranasally, buccally, rectally or topically, for example to the skin, the mucous membranes or the eyes. For oral application suitable preparations are in the form of tablets, sugar-coated pills, capsules, granules, droplets, juices and syrups, while for parenteral, topical and inhalative application suitable forms are solutions, suspensions, readily reconstitutable dry preparations, as well as sprays. Form A in a depot form, in dissolved form or in a plaster, optionally with the addition of agents promoting skin penetration, are suitable percutaneous application preparations. Preparation forms that can be administered orally or percutaneously can provide for the delayed release of crystalline Form A according to the invention. In principle further active constituents known to the person skilled in the art may be added to the medicaments according to the invention.

Preferred formulations for crystalline Form A (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride according to the invention are presented in the PCT-application WO 03/035054 incorporated herein by reference.

The amount of active constituent to be administered to the patient varies depending on the patient's weight, on the type of application, medical indication and severity of the condition. Normally 0.005 to 1000 mg/kg, preferably 0.05 to 5 mg/kg of crystalline Form A according to the invention are administered.

Preferably, the crystalline Form A according to the invention is used for the treatment of pain or the treatment of urinary incontinence. Accordingly the invention also relates to the use of crystalline Form A according to the invention for the treatment of pain or the treatment of urinary incontinence.

Additionally the invention relates to a method of treatment using a sufficient amount of crystalline Form A according to the invention for the treatment of a disease, especially pain or urinary incontinence.

Certain embodiments of the present invention may be further understood by reference to the following specific examples. These examples and the terminology used herein are for the purpose of describing particular embodiments only and are not intended to be limiting.

Example 1: Master Recipe for Preparation of Form A

The master recipe is valid for a 50 ml scale.

Provide 1.9 g (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride prepared according to example 25 of European Patent EP 693 475 B1 in a 50 ml glass round bottom vessel with a 3-blade overhead stirrer with baffles.

Add 25 ml isopropanol and 0.5% (v/v) water

Stir at 800 rpm

Heat to 80° C.

Hold temperature while stirring for 10 minutes

Cool to 65° C.

Add 0.056 g seeds (Mean Sq. Wt. CL=58 μm², Median No Wt. CL=22 μm)

Cool to 0° C. over 1 hour

Filter slurry through PTFE filter column (5 μm pore size)

Dry solid material under slight vacuum until constant weight (approx. 24 hours)

Repeat the same procedure with the dry solid material obtained

Example 2: Preparation of Form A (1)

(−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride was prepared according to example 25 of European Patent EP 693 475 B1. 32.2 mg of the thus synthesized (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride was—by slight heating up to 40° C. and/or agitating on an orbital shaker for 30 min—dissolved in 20 ml acetone. Following that the solution was filtered through a nylon syringe filter having a mesh of 0.20 μm and the solution was left to crystallize by slow evaporation of the solvent. Crystalline Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride was generated as proven by X-ray powder diffraction and by RAMAN microscopic analysis.

Example 3: Preparation of Form A (2)

(−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride was prepared according to example 25 of European Patent EP 693 475 B1. 32.2 mg of the thus synthesized (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride was—if necessary by agitating for e.g. 30 min—dissolved in 20 ml acetone. Following that the solution was filtered with a nylon syringe filter having a mesh of 0.20 μm and the solution was left to crystallize by slow evaporation of the solvent. In no step after and including the dissolving the temperature was allowed to rise above +25° C. Crystalline Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride was generated as proven by X-ray powder diffraction experiment and by RAMAN microscopic analysis.

Example 4: Preparation of Form A (3)

(−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride was prepared according to example 25 of European Patent EP 693 475 B1. 350 mg of the thus synthesized (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride were dissolved in 50 ml acetonitrile in a 250 ml flask. The mixture was stirred for 1.5 h on a water bath heated to 37° C.±1° C. Any insoluble residue was removed by filtering. Of the clear solution 35 ml was removed on a rotation evaporator at 70-80 mbar and a temperature of the water bath of 30° C.±1° C. The precipitated solid compound was filtered by vacuum. Crystalline Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride was generated as proven by X-ray powder diffraction and by RAMAN microscopic analysis.

Example 5: Preparation of Form A (4)

(−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride was prepared according to example 25 of European Patent EP 693 475 B1. The thus synthesized (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride was stored for 72 h at −40° C. Crystalline Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride was generated as proven by X-ray powder diffraction and by RAMAN microscopic analysis.

Example 6: Preparation of Form A (5)

(−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride was prepared according to example 25 of European Patent EP 693 475 B1. 370 mg of the thus synthesized (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride were added to 40 ml acetonitrile and 100 mg active carbon in a 100 ml flask and heated to the boiling point. The active carbon was filtered off from the hot solution by means of a paper filter and the filtrate concentrated to a volume of approx. 10 ml in a rotation evaporator at 150±10 mbar and 50° C. The solution was slowly rotated for 30 minutes at room temperature. Following that the solution was allowed to stand for 30 minutes at room temperature and than for 1 hour at 4° C. The Crystals are filtered by vacuum through a glass filter (276 mg yield).

266 mg of these Crystals were dissolved at room temperature in 45 ml acetonitrile, insoluble residues were removed by filtration and the solution was rotated for 1.5 h at 35-40° C. at atmospheric pressure in a rotation evaporator. Than the solution was concentrated at 50° C. and 150±10 mbar to a volume of approx. 10 ml and then slowly rotated for 30 minutes at room temperature. Following that the flask was allowed to stand for 12 h at 4° C.

The precipitated solid is filtered by vacuum through a glass filter and dried in the air.

Yield:

151 mg (40.8% of the theory in relation to used educt), white microcrystalline solid form

Example 7: Preparation of Form B (1)

(−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride was prepared according to example 25 of European Patent EP 693 475 B1. Crystalline Form B of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride was generated as proven by X-ray powder diffraction and by RAMAN microscopic analysis.

Example 8: Preparation of Form B (2)

(−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride prepared according to one of the examples 1 to 5 was milled for at least 20 min. Then it was kept at 130° C. in an oven for 80 min. Crystalline Form B of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride was generated as proven by X-ray powder diffraction and by RAMAN microscopic analysis.

Example 9: Preparation of Form B (3)

(−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride prepared according to one of the examples 1 to 5 was cryogrinded for at least 15 min. Then it was kept at 125° C. in a TGA for 30 min. Crystalline Form B of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride was generated as proven by X-ray powder diffraction and by RAMAN microscopic analysis.

Example 10: X-ray Powder Diffraction Patterns of Forms A (1) and B (1)

Powder Data Collection was performed with a STOE Stadi P Transmission Powder Diffractometer equipped with a curved germanium monochromator and a linear position sensitive detector. The very carefully ground powders were prepared as flat samples. As source of the beam a copper X-ray tube with monochromatized Cu Kai (λ=1.54051 Å) radiation generated at 50 kV and 30 mA was used. The 20 area for the measurement was 5°-40°. The used step width was 0.02 degrees in 2 theta. The data were collected at a temperature of 23±1°.

The X-ray pattern for Form A is shown in FIG. 1, the X-ray pattern for Form B in FIG. 4.

The data are shown in Table 1.

TABLE 1 Peak and Relative Intensity Listing (°2θ, peaks with I/I1 value of 10 and over) Peak No. A I/I1 B I/I1 1 9.07 10 14.58 100 2 10.11 9 14.94 9 3 14.51 100 15.42 19 4 15.08 24 15.76 27 5 15.39 11 16.05 8 6 15.69 22 16.77 14 7 15.96 24 18.01 60 8 16.62 13 19.60 39 9 17.00 20 20.18 27 10 18.24 63 20.98 19 11 18.88 28 21.43 14 12 20.00 23 21.99 65 13 20.39 47 23.71 4 14 21.66 47 24.73 43 15 22.54 41 25.10 14 16 24.27 28 25.71 21 17 25.03 13 26.29 10 18 25.47 43 26.81 5 19 25.84 20 27.76 20 20 26.04 27 28.19 39 21 26.94 13 29.20 12 22 27.29 29 29.86 13 23 27.63 28 30.28 5 24 28.33 20 30.58 6 25 28.72 12 31.15 22 26 29.09 12 32.41 6 27 29.29 21 32.91 5 28 29.76 11 33.17 6 29 30.37 23 34.34 6 30 30.74 11 35.88 9 31 31.70 14 36.29 7 32 34.37 11 39.08 9

Example 11: IR Spectrum of Forms A and B

The mid IR spectra were acquired on a Nicolet model 860 Fourier transform IR spectrophotometer equipped with a globar source, Ge/KBr beamsplitter, and deterated triglycine sulfate (DTGS) detector. A Spectra-Tech, Inc. diffuse reflectance accessory was utilized for sampling. Each spectrum represents 256 co-added scans at a spectral resolution of 4 cm⁻¹. A background data set was then acquired with an alignment mirror in place. A single beam sample data set was then acquired. Subsequently, a Log 1/R (R=Reflectance) spectrum was acquired by rationing the two data sets against each other. The spectrophotometer was calibrated (wavelength) with polystyrene at the time of use.

The spectrum for Form A is shown in FIG. 2. The spectrum for Form B is shown in FIG. 5.

The data are shown in the following Table 2.

TABLE 2 IR Peak Listing Form A Form B Peak Pos. Intensity Peak Pos. Intensity (cm⁻¹) (log 1/R) (cm⁻¹) (log 1/R) 3180.4 1.878 3170.2 2.196 2970 1.856 3013.1 1.791 1462.1 1.848 2962.5 2.098 2695.2 1.841 2933.4 1.945 1600.9 1.838 2682 2.116 1281.6 1.771 1940.5 1.242 1378.3 1.763 1870.7 1.246 1219.9 1.754 1801.7 1.201 1181.2 1.748 1749.5 1.236 1503.6 1.743 1598.1 2.138 1256.5 1.734 1503.2 1.755 712.6 1.725 1451.5 2.164 879.8 1.713 1417.2 1.89 684.7 1.692 1396.3 1.843 798.7 1.681 1377.1 1.864 1313.6 1.673 1353.2 1.726 1005.1 1.655 1313.2 1.661 731.2 1.63 1280.7 1.977 1090.9 1.626 1254.8 1.973 810.2 1.622 1217.6 2.015 971.5 1.588 1177.5 1.868 842.6 1.576 1154.6 1.597 831.7 1.574 1136.4 1.431 1111.5 1.55 1111.3 1.512 1049.8 1.534 1090.3 1.625 1136.5 1.498 1065.9 1.425 461.3 1.476 1049.9 1.52 1065.8 1.457 1004.6 1.813 495.1 1.438 958.7 1.855 542.1 1.408 946.6 1.735 595.8 1.384 912.5 1.292 527.9 1.327 877.8 1.951 912.4 1.304 842.7 1.657 1032.4 1.3 831.4 1.664 416.9 1.287 810.7 1.715 1698.3 1.282 795.2 1.892 1940.5 1.279 730.6 1.855 1870.6 1.277 711.7 2.04 1749.4 1.268 683.4 1.917 1801.6 1.208 595.6 1.439 2115.5 1.061 542.1 1.497 527.7 1.425 495.1 1.663 464.4 1.622 416.7 1.439

Example 12: Single Crystal Structure Analysis of Form A

A colorless crystal of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methyl-propyl)-phenol hydrochloride prepared according to one of the examples 2 to 6 having approximate dimensions of 0.6×0.60×0.50 mm was mounted on a glass fiber in random orientation. Preliminary examination and data collection were performed with Cu K_(α) radiation (1.54184 Å) on a Enraf-Nonius CAD4 computer controlled kappa axis diffractometer equipped with a graphite crystal, incident beam monochromator.

Cell constants and an orientation matrix for data collection were obtained from least-squares refinement using the setting angles of 25 reflections in the range 16°<θ<24°, measured by the computer controlled diagonal slit method of centering. The monoclinic cell parameters and calculated volume are:

a=7.110(3), b=11.615(4), c=17.425(6) Å, β=95.00(3), V=1433.5(10) Å³. For Z=4 and formula weight of 257.79 the calculated density is 1.20 g·cm⁻³. The space group was determined to be P2₁ (No. 19).

The data were collected at a temperature of −103±5° C. using ω-θ scan technique. The scan rate varied from 4 to 20°/min (in ω). The variable scan rate allows rapid data collection for intense reflections where a fast scan rate is used and assures good counting statistics for weak reflections where a slow scan rate is used. Data were collected to a maximum of 2θ of 75.11°. The scan range) (in°) was determined as a function of θ to correct for the separation of the Kα doublet. The scan width was calculated as follows:

θ scan width=0.8+0.140 tan θ

Moving-crystal moving-counter background counts were made by scanning an additional 25% above and below this range. Thus the ratio of peak counting time to background counting time was 2:1. The counter aperture was also adjusted as a function of θ. The horizontal aperture width ranged from 2.4 to 2.5 mm; the vertical aperture was set at 4.0 mm.

The data for Form A as collected in a commonly known “.cif”-document for complete reference of distances within the molecule are shown in Table 3.

TABLE 3 Table 3a. Crystal data and structure refinement for Form_A. Identification code FormA Empirical formula C14 H24 Cl N O Formula weight 257.79 Temperature 170(2) K Wavelength 1.54184 Å Crystal system monoclinic Space group P 21 Unit cell dimensions a = 7.110(3) Å alpha = 90 deg. b = 11.615(4) Å beta = 95.00(3) deg. c = 17.425(6) Å gamma = 90 deg. Volume 1433.5(10) Å³ Z 4 Density (calculated) 1.195 Mg/m³ Absorption coefficient 2.230 mm⁻¹ F(000) 560 Theta range for data collection 4.58 to 75.11 deg. Index ranges 0 <= h <= 8, −14 <= k <= 14, −21 <= l <= 21 Reflections collected 4531 Independent reflections 4531 [R(int) = 0.0000] Refinement method Full-matrix least-squares on F² Data/restraints/parameters 4531/1/323 Goodness-of-fit on F² 1.035 Final R indices [I > 2sigma(I)] R1 = 0.0588, wR2 = 0.1629 R indices (all data) R1 = 0.0643, wR2 = 0.1673 Absolute structure parameter .027(19) Largest diff. peak and hole 0.686 and −0.696 e.Å⁻³ Table 3b. Atomic coordinates (×10⁴) and equivalent isotropic displacement parameters (Å² × 10³) for Form_A. U(eq) is defined as one third of the trace of the orthogonalized Uij tensor. x y z U(eq) Cl(1)    2148(1)   3541(1)  9878(1) 29(1) Cl(2)    7279(1)   2551(1)  5089(1) 28(1) O(1)  −588(5)   5289(3)  9077(2) 36(1) N(1)    822(4)   3979(3)  4964(2) 22(1) O(2)    4799(4)    769(3)  5795(2) 36(1) N(2)    5722(5)   2083(3) 10053(2) 27(1) C(1)    2263(6)   3215(4)  4667(2) 33(1) C(2)   −85(6)   4736(4)  4336(2) 31(1) C(3)    1580(5)   4713(3)  5628(2) 22(1) C(4)    2627(5)   4056(3)  6291(2) 21(1) C(5)    1401(6)   3130(4)  6613(2) 29(1) C(6)    3437(5)   4902(3)  6925(2) 22(1) C(7)    4927(5)   5729(4)  6656(2) 27(1) C(8)    6603(6)   5138(4)  6351(3) 38(1) C(9)    1930(5)   5552(3)  7326(2) 21(1) C(10)    1188(6)   6603(3)  7050(2) 25(1) C(11)  −137(6)   7175(3)  7448(2) 28(1) C(12)  −739(6)   6733(4)  8117(2) 28(1) C(13)   −19(6)   5686(4)  8404(2) 26(1) C(14)    1313(5)   5102(3)  8001(2) 23(1) C(20)    7093(7)   2841(5) 10502(3) 41(1) C(21)    4877(7)   1235(5) 10570(3) 41(1) C(22)    6542(6)   1458(3)  9408(2) 25(1) C(23)    7484(5)   2230(3)  8856(2) 22(1) C(24)    6086(6)   3070(4)  8447(2) 29(1) C(25)    8541(5)   1512(3)  8274(2) 20(1) C(26)   10222(6)    857(4)  8681(2) 28(1) C(27)   11528(6)    374(4)  8118(3) 36(1) C(28)    7250(5)    740(3)  7756(2) 22(1) C(29)    6682(5)  −349(3)  7991(2) 24(1) C(30)    5507(5) −1019(3)  7501(2) 26(1) C(31)    4871(6)  −654(3)  6769(2) 26(1) C(32)    5427(6)    430(4)  6529(2) 26(1) C(33)    6604(5)   1116(4)  7018(2) 24(1) Table 3c. Bond lengths [A] and angles [deg] for Form_A. O(1)—C(13) 1.355(5) O(1)—H(1)  .86(11) N(1)—C(1) 1.482(5) N(1)—C(3) 1.499(5) N(1)—C(2) 1.504(5) N(1)—H(1A)   .9100 O(2)—C(32) 1.374(5) O(2)—H(2)  .90(9) N(2)—C(20) 1.485(6) N(2)—C(21) 1.495(6) N(2)—C(22) 1.497(5) N(2)—H(2A)   .9100 C(1)—H(1A)   .9801 C(1)—H(1B)   .9801 C(1)—H(1C)   .9801 C(2)—H(2A)   .9801 C(2)—H(2B)   .9801 C(2)—H(2C)   .9801 C(3)—C(4) 1.524(5) C(3)—H(3A)   .9800 C(3)—H(3B)   .9800 C(4)—C(5) 1.522(5) C(4)—C(6) 1.553(5) C(4)—H(4)   .9800 C(5)—H(5A)   .9801 C(5)—H(5B)   .9801 C(5)—H(5C)   .9801 C(6)—C(9) 1.528(5) C(6)—C(7) 1.533(6) C(6)—H(6)   .9800 C(7)—C(8) 1.511(6) C(7)—H(7A)   .9800 C(7)—H(7B)   .9800 C(8)—H(8A)   .9801 C(8)—H(8B)   .9801 C(8)—H(8C)   .9801 C(9)—C(14) 1.392(5) C(9)—C(10) 1.398(5) C(10)—C(11) 1.386(6) C(10)—H(10)   .9800 C(11)—C(12) 1.376(6) C(11)—H(11)   .9800 C(12)—C(13) 1.395(6) C(12)—H(12)   .9800 C(13)—C(14) 1.402(5) C(14)—H(14)   .9800 C(20)—H(20A)   .9801 C(20)—H(20B)   .9801 C(20)—H(20C)   .9801 C(21)—H(21A)   .9801 C(21)—H(21B)   .9801 C(21)—H(21C)   .9801 C(22)—C(23) 1.513(5) C(22)—H(22A)   .9800 C(22)—H(22B)   .9800 C(23)—C(24) 1.525(5) C(23)—C(25) 1.556(5) C(23)—H(23)   .9800 C(24)—H(24A)   .9801 C(24)—H(24B)   .9801 C(24)—H(24C)   .9801 C(25)—C(28) 1.523(5) C(25)—C(26) 1.537(5) C(25)—H(25)   .9800 C(26)—C(27) 1.517(5) C(26)—H(26A)   .9800 C(26)—H(26B)   .9800 C(27)—H(27A)   .9801 C(27)—H(27B)   .9801 C(27)—H(27C)   .9801 C(28)—C(33) 1.397(5) C(28)—C(29) 1.400(6) C(29)—C(30) 1.382(6) C(29)—H(29)   .9800 C(30)—C(31) 1.381(6) C(30)—H(30)   .9800 C(31)—C(32) 1.395(6) C(31)—H(31)   .9800 C(32)—C(33) 1.392(6) C(33)—H(33)   .9800 C(13)—O(1)—H(1)   116(6) C(1)—N(1)—C(3) 113.4(3) C(1)—N(1)—C(2) 111.2(3) C(3)—N(1)—C(2) 109.4(3) C(1)—N(1)—H(1A) 107.5 C(3)—N(1)—H(1A) 107.5 C(2)—N(1)—H(1A) 107.5 C(32)—O(2)—H(2)   127(6) C(20)—N(2)—C(21) 110.7(4) C(20)—N(2)—C(22) 113.7(3) C(21)—N(2)—C(22) 109.6(3) C(20)—N(2)—H(2A) 107.5 C(21)—N(2)—H(2A) 107.5 C(22)—N(2)—H(2A) 107.5 N(1)—C(1)—H(1A) 109.5 N(1)—C(1)—H(1B) 109.5 H(1A)—C(1)—H(1B) 109.5 N(1)—C(1)—H(1C) 109.5 H(1A)—C(1)—H(1C) 109.5 H(1B)—C(1)—H(1C) 109.5 N(1)—C(2)—H(2A) 109.5 N(1)—C(2)—H(2B) 109.5 H(2A)—C(2)—H(2B) 109.5 N(1)—C(2)—H(2C) 109.5 H(2A)—C(2)—H(2C) 109.5 H(2B)—C(2)—H(2C) 109.5 N(1)—C(3)—C(4) 114.8(3) N(1)—C(3)—H(3A) 108.6 C(4)—C(3)—H(3A) 108.6 N(1)—C(3)—H(3B) 108.6 C(4)—C(3)—H(3B) 108.6 H(3A)—C(3)—H(3B) 107.6 C(5)—C(4)—C(3) 112.1(3) C(5)—C(4)—C(6) 111.9(3) C(3)—C(4)—C(6) 110.4(3) C(5)—C(4)—H(4) 107.4 C(3)—C(4)—H(4) 107.4 C(6)—C(4)—H(4) 107.4 C(4)—C(5)—H(5A) 109.5 C(4)—C(5)—H(5B) 109.5 H(5A)—C(5)—H(5B) 109.5 C(4)—C(5)—H(5C) 109.5 H(5A)—C(5)—H(5C) 109.5 H(5B)—C(5)—H(5C) 109.5 C(9)—C(6)—C(7) 111.2(3) C(9)—C(6)—C(4) 114.0(3) C(7)—C(6)—C(4) 113.7(3) C(9)—C(6)—H(6) 105.7 C(7)—C(6)—H(6) 105.7 C(4)—C(6)—H(6) 105.7 C(8)—C(7)—C(6) 114.2(4) C(8)—C(7)—H(7A) 108.7 C(6)—C(7)—H(7A) 108.7 C(8)—C(7)—H(7B) 108.7 C(6)—C(7)—H(7B) 108.7 H(7A)—C(7)—H(7B) 107.6 C(7)—C(8)—H(8A) 109.5 C(7)—C(8)—H(8B) 109.5 H(8A)—C(8)—H(8B) 109.5 C(7)—C(8)—H(8C) 109.5 H(8A)—C(8)—H(8C) 109.5 H(8B)—C(8)—H(8C) 109.5 C(14)—C(9)—C(10) 118.7(3) C(14)—C(9)—C(6) 119.0(3) C(10)—C(9)—C(6) 122.2(3) C(11)—C(10)—C(9) 119.9(4) C(11)—C(10)—H(10) 120.0 C(9)—C(10)—H(10) 120.0 C(12)—C(11)—C(10) 121.3(4) C(12)—C(11)—H(11) 119.3 C(10)—C(11)—H(11) 119.3 C(11)—C(12)—C(13) 119.8(4) C(11)—C(12)—H(12) 120.1 C(13)—C(12)—H(12) 120.1 O(1)—C(13)—C(12) 118.6(4) O(1)—C(13)—C(14) 122.3(4) C(12)—C(13)—C(14) 119.0(4) C(9)—C(14)—C(13) 121.2(3) C(9)—C(14)—H(14) 119.4 C(13)—C(14)—H(14) 119.4 N(2)—C(20)—H(20A) 109.5 N(2)—C(20)—H(20B) 109.5 H(20A)—C(20)—H(20B) 109.5 N(2)—C(20)—H(20C) 109.5 H(20A)—C(20)—H(20C) 109.5 H(20B)—C(20)—H(20C) 109.5 N(2)—C(21)—H(21A) 109.5 N(2)—C(21)—H(21B) 109.5 H(21A)—C(21)—H(21B) 109.5 N(2)—C(21)—H(21C) 109.5 H(21A)—C(21)—H(21C) 109.5 H(21B)—C(21)—H(21C) 109.5 N(2)—C(22)—C(23) 114.4(3) N(2)—C(22)—H(22A) 108.7 C(23)—C(22)—H(22A) 108.7 N(2)—C(22)—H(22B) 108.7 C(23)—C(22)—H(22B) 108.7 H(22A)—C(22)—H(22B) 107.6 C(22)—C(23)—C(24) 111.7(3) C(22)—C(23)—C(25) 111.3(3) C(24)—C(23)—C(25) 111.8(3) C(22)—C(23)—H(23) 107.3 C(24)—C(23)—H(23) 107.3 C(25)—C(23)—H(23) 107.3 C(23)—C(24)—H(24A) 109.5 C(23)—C(24)—H(24B) 109.5 H(24A)—C(24)—H(24B) 109.5 C(23)—C(24)—H(24C) 109.5 H(24A)—C(24)—H(24C) 109.5 H(24B)—C(24)—H(24C) 109.5 C(28)—C(25)—C(26) 112.8(3) C(28)—C(25)—C(23) 113.7(3) C(26)—C(25)—C(23) 111.4(3) C(28)—C(25)—H(25) 106.1 C(26)—C(25)—H(25) 106.1 C(23)—C(25)—H(25) 106.1 C(27)—C(26)—C(25) 112.3(3) C(27)—C(26)—H(26A) 109.1 C(25)—C(26)—H(26A) 109.1 C(27)—C(26)—H(26B) 109.1 C(25)—C(26)—H(26B) 109.1 H(26A)—C(26)—H(26B) 107.9 C(26)—C(27)—H(27A) 109.5 C(26)—C(27)—H(27B) 109.5 H(27A)—C(27)—H(27B) 109.5 C(26)—C(27)—H(27C) 109.5 H(27A)—C(27)—H(27C) 109.5 H(27B)—C(27)—H(27C) 109.5 C(33)—C(28)—C(29) 118.2(4) C(33)—C(28)—C(25) 119.6(3) C(29)—C(28)—C(25) 122.2(3) C(30)—C(29)—C(28) 120.1(4) C(30)—C(29)—H(29) 120.0 C(28)—C(29)—H(29) 120.0 C(31)—C(30)—C(29) 122.0(4) C(31)—C(30)—H(30) 119.0 C(29)—C(30)—H(30) 119.0 C(30)—C(31)—C(32) 118.4(4) C(30)—C(31)—H(31) 120.8 C(32)—C(31)—H(31) 120.8 O(2)—C(32)—C(31) 117.4(4) O(2)—C(32)—C(33) 122.3(4) C(31)—C(32)—C(33) 120.3(4) C(28)—C(33)—C(32) 121.1(4) C(28)—C(33)—H(33) 119.5 C(32)—C(33)—H(33) 119.5 Symmetry transformations used to generate equivalent atoms: Table 3d. Hydrogen coordinates (×10⁴) and isotropic displacement parameters (Å² × 10³) for Form_A. x y z U(eq) H(1)  −380(15)   4570(10)  9180(5) 110(3) H(1A)   −96   3523  5133  26 H(2)    5310(14)   1310(9)  5510(5) 100(3) H(2A)    4770   2536  9841  32 H(1A)    1737   2848  4189  43 H(1B)    2630   2622  5051  43 H(1C)    3374   3671  4564  43 H(2A)    838   5299  4182  41 H(2B)  −1162   5141  4525  41 H(2C)  −523   4261  3891  41 H(3A)    525   5130  5827  29 H(3B)    2438   5287  5439  29 H(4)    3700   3668  6086  27 H(5A)    2110   2747  7048  38 H(5B)    1040   2563  6210  38 H(5C)    262   3484  6788  38 H(6)    4100   4422  7324  28 H(7A)    4328   6227  6252  35 H(7B)    5381   6223  7090  35 H(8A)    7580   5710  6270  49 H(8B)    6204   4761  5860  49 H(8C)    7111   4561  6723  49 H(10)    1604   6936  6577  32 H(11)  −656   7908  7248  36 H(12)  −1670   7153  8392  36 H(14)    1819   4364  8198  30 H(20A)    6484   3193 10927  54 H(20B)    7521   3445 10166  54 H(20C)    8179   2384 10710  54 H(21A)    4403   1642 11006  53 H(21B)    5842    677 10760  53 H(21C)    3833    830 10281  53 H(22A)    5532   1026  9118  32 H(22B)    7472    900  9629  32 H(23)    8433   2688  9162  29 H(24A)    5114   2639  8133  38 H(24B)    6755   3580  8115  38 H(24C)    5491   3530  8830  38 H(25)    9081   2070  7933  26 H(26A)   10938   1379  9040  37 H(26B)    9748    224  8982  37 H(27A)   10856  −210  7794  46 H(27B)   12632    24  8403  46 H(27C)   11941    997  7792  46 H(29)    7118  −637  8505  31 H(30)    5114 −1776  7677  34 H(31)    4048 −1144  6428  34 H(33)    6986   1876  6842  31 Table 3e. Anisotropic displacement parameters (Å² × 10³) for Form_A. The anisotropic displacement factor exponent takes the form: −2 pi² [ h² a*² U11 + . . . + 2 h k a* b* U12 ] U11 U22 U33 U23 U13 U12 C1(1) 23(1) 27(1) 36(1)  −3(1)  −1(1)    4(1) C1(2) 23(1) 25(1) 35(1)  −2(1)  −2(1)  −5(1) O(1) 35(2) 41(2) 33(2)    7(1)    8(1)   13(1) N(1) 19(2) 28(2) 18(1)    1(1)  −4(1)  −5(1) O(2) 33(2) 52(2) 21(1)    5(1) −11(1) −12(2) N(2) 22(2) 31(2) 27(2)    2(1)    2(1)    8(1) C(1) 29(2) 44(2) 26(2)  −6(2)    1(2)    6(2) C(2) 25(2) 41(2) 26(2)   11(2)  −8(2)  −4(2) C(3) 20(2) 20(2) 26(2)    2(1)  −4(1)  −4(1) C(4) 19(2) 23(2) 20(2)  −1(1)  −2(1)    3(1) C(5) 33(2) 25(2) 28(2)    2(2)  −3(2)  −4(2) C(6) 17(2) 26(2) 20(2)  −2(1)  −6(1)    6(1) C(7) 18(2) 30(2) 32(2) −10(2)  −6(1)    0(2) C(8) 20(2) 40(2) 54(3) −11(2)    5(2)  −3(2) C(9) 18(2) 26(2) 19(2)  −6(1)  −7(1)    1(1) C(10) 23(2) 24(2) 26(2)    0(2)  −4(1)    1(1) C(11) 23(2) 28(2) 32(2)    0(2)  −9(2)    5(2) C(12) 20(2) 31(2) 32(2)  −5(2)  −1(2)    5(2) C(13) 22(2) 33(2) 24(2)    0(2)  −2(1)    3(2) C(14) 20(2) 24(2) 25(2)    0(2)  −5(1)    5(1) C(20) 40(3) 51(3) 32(2) −12(2)  −3(2)  −1(2) C(21) 39(3) 49(3) 37(2)   10(2)   16(2)   10(2) C(22) 27(2) 23(2) 25(2)  −1(2)    2(2)    2(2) C(23) 21(2) 22(2) 22(2)  −2(1)  −3(1)    2(1) C(24) 32(2) 27(2) 27(2)    2(2)  −1(2)    8(2) C(25) 15(2) 24(2) 20(2)    1(1)  −3(1)    1(1) C(26) 21(2) 33(2) 30(2)  −2(2)  −4(2)    6(2) C(27) 25(2) 39(2) 43(2)    1(2)    4(2)    7(2) C(28) 18(2) 27(2) 21(2)  −1(2)    1(1)    5(1) C(29) 22(2) 25(2) 25(2)  −1(2)    1(1)    3(1) C(30) 24(2) 22(2) 33(2)  −4(2)    6(2)  −1(2) C(31) 19(2) 31(2) 28(2) −10(2)    1(1)  −2(2) C(32) 21(2) 35(2) 21(2)  −2(2)    2(1)  −2(2) C(33) 17(2) 30(2) 25(2)    1(2)    1(1)  −4(1)

Example 13: Single Crystal Structure Analysis of Form B

A colorless chunk of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride prepared according to one of the examples 7 to 9 having approximate dimensions of 0.44×0.40×0.35 mm was mounted on a glass fiber in random orientation. Preliminary examination and data collection were performed with Mo K_(α) radiation (λ=0.71073 Å) on a Nonius KappaCCD diffractometer.

Cell constants and an orientation matrix for data collection were obtained from least-squares refinement using the setting angles of 6172 reflections in the range 5<θ<27°. The orthorhombic cell parameters and calculated volume are: a=7.0882(3), b=11.8444(6), c=17.6708(11) Å, V=1483.6(2) Å³. For Z=4 and formula weight of 257.79 the calculated density is 1.15 g·cm⁻³. The refined mosaicity from DENZO/SCALEPACK was 0.68° (<1 mod, <2 poor) indicating moderate crystal quality. The space group was determined by the program ABSEN. From the systematic presence of:

-   -   h00 h=2n     -   0k0 k=2n     -   001 1=2n         and from subsequent least-squares refinement, the space group         was determined to be P2₁2₁2₁ (number 19).

The data were collected to a maximum 2θ value of 55.0°, at a temperature of 343±1 K.

The data from examples 12 and 13 are compared in Table 3f:

TABLE 3f Form A (monoklin) Form B (orthorhombic) Formula C14 H24 Cl N O C14 H24 Cl N O M.W./g/mol 257.79 257.79 Space group No. 4, P2₁ No. 19, P2₁2₁2₁ Z (No. of Units) 4 4 a/Å  7.110(3) 7.0882(3) b/Å 11.615(4) 11.8444(6)  c/Å 17.425(6) 17.6708(11) α/° 90 90 β/°  95.00(3) 90 γ/° 90 90 Volume of elementary 1434 1484 cell/Å³ Density (calc.)/g/cm³ 1.20 1.15

The data for Form B as collected in a commonly known “.cif”-document for complete reference of distances within the molecule are shown below Table 4:

TABLE 4 Table 4a. Crystal data and structure refinement for Form_B. Identification code FormB Empirical formula C14 H2 H22 Cl N O Formula weight 257.79 Temperature 343 K Wavelength .71073 Å Crystal system orthorhombic Space group P 21 21 21 Unit cell dimensions a = 7.0882(3) Å alpha = 90 deg. b = 11.8444(6) Å beta = 90 deg. c = 17.6708(11) Å gamma = 90 deg. Volume 1483.56(13) Å³ Z 4 Density (calculated) 1.154 Mg/m³ Absorption coefficient 0.244 mm⁻¹ F(000) 560 Theta range for data collection 5.04 to 27.49 deg. Index ranges −9 <= h <= 9, −15 <= k <= 15, −22 <= l <= 22 Reflections collected 3207 Independent reflections 3207 [R(int) = 0.0000] Refinement method Full-matrix least-squares on F² Data/restraints/parameters 3207/0/167 Quality-of-fit on F² 1.012 Final R indices [I > 2sigma(I) ] R1 = 0.0440, wR2 = 0.1137 R indices (all data) R1 = 0.0598, wR2 = 0.1246 Absolute structure parameter −.03(8) Extinction coefficient .033(7) Largest diff. peak and hole 0.265 and -0.202 e.Å⁻³ Table 4b. Atomic coordinates (×10⁴) and equivalent isotropic displacement parameters (Å² × 10³) for Form_B. U(eq) is defined as one third of the trace of the orthogonalized Uij tensor. x Y z U(eq) Cl  7978(1) −1959(1) 7646(1) 74(1) O(33)  4870(3)    85(2) 3443(1) 94(1) N(6)  5522(3)   1571(2) 7545(1) 64(1) C(1) 11558(4)  −160(3) 5596(2) 98(1) C(2) 10168(3)    333(2) 6149(2) 75(1) C(3)  8514(3)    925(2) 5758(1) 58(1) C(4)  7395(3)   1654(2) 6327(1) 58(1) C(5)  6394(3)    922(2) 6909(1) 64(1) C(6)  4611(5)    782(3) 8089(2) 96(1) C(7)  6834(5)   2342(3) 7943(2) 95(1) C(31)  7273(3)    131(2) 5286(1) 57(1) C(32)  6643(3)    472(2) 4583(1) 61(1) C(33)  5509(3)  −219(2) 4138(1) 68(1) C(34)  5050(3) −1291(2) 4395(2) 74(1) C(35)  5679(4) −1637(2) 5098(2) 75(1) C(36)  6782(3)  −946(2) 5542(1) 66(1) C(41)  6029(4)   2461(2) 5931(2) 80(1) Table 4c. Bond lengths [Å] and angles for Form_B. O(33)—H(33)   .76(3) O(33)—C(33)  1.358(3) N(6)—H(6)   .82(2) N(6)—C(7)  1.481(4) N(6)—C(6)  1.488(3) N(6)—C(5)  1.496(3) C(1)—C(2)  1.505(4) C(2)—C(3)  1.531(3) C(3)—C(31)  1.534(3) C(3)—C(4)  1.546(3) C(4)—C(5)  1.520(3) C(4)—C(41)  1.530(3) C(31)—C(32)  1.381(3) C(31)—C(36)  1.396(3) C(32)—C(33)  1.391(3) C(33)—C(34)  1.387(4) C(34)—C(35)  1.382(4) C(35)—C(36)  1.377(4) H(33)—O(33)—C(33)   118(3) H(6)—N(6)—C(7)  104.9(15) H(6)—N(6)—C(6)  108.8(16) C(7)—N(6)—C(6)  110.7(2) H(6)—N(6)—C(5)  107.8(16) C(7)—N(6)—C(5)  114.5(2) C(6)—N(6)—C(5)  110.0(2) C(1)—C(2)—C(3)  112.7(3) C(2)—C(3)—C(31)  113.8(2) C(2)—C(3)—C(4)  110.8(2) C(31)—C(3)—C(4) 113.71(16) C(5)—C(4)—C(41) 111.75(18) C(5)—C(4)—C(3) 111.13(17) C(41)—C(4)—C(3) 112.08(19) N(6)—C(5)—C(4) 114.03(18) C(32)—C(31)—C(36)  118.5(2) C(32)—C(31)—C(3) 119.66(19) C(36)—C(31)—C(3)  121.8(2) C(31)—C(32)—C(33)  121.6(2) O(33)—C(33)—C(34)  117.5(2) O(33)—C(33)—C(32)  123.2(2) C(34)—C(33)—C(32)  119.3(2) C(35)—C(34)—C(33)  119.3(2) C(36)—C(35)—C(34)  121.2(2) C(35)—C(36)−C(31)  120.0(2) Symmetry transformations used to generate equivalent atoms: Table 4d. Hydrogen coordinates (×10⁴) and isotropic displacement parameters (Å² × 10³) for Form_B. x y z U(eq) H(33)  5160(4)    660(2) 3290(2)  80(10) H(6)  4710(3)   1983(17) 7365(13)  54(6) H(1A) 10962  −753 5313 148 H(1B) 12620  −460 5867 148 H(1C) 11980    419 5256 148 H(2A) 10815    871 6472  90 H(2B)  9682  −266 6469  90 H(3)  9079   1455 5398  70 H(4)  8312   2119 6602  70 H(5A)  5415    492 6655  76 H(5B)  7293    388 7117  76 H(6A)  3594    393 7842 144 H(6B)  4128   1200 8512 144 H(6C)  5524    243 8264 144 H(7A)  7907   1923 8120 143 H(7B)  6200   2680 8366 143 H(7C)  7246   2922 7601 143 H(32)  6984   1181 4403  74 H(34)  4325 −1772 4097  88 H(35)  5352 −2351 5274  90 H(36)  7200 −1195 6012  79 H(41A)  5030   2036 5700 120 H(41B)  6693   2879 5549 120 H(41C)  5506   2975 6295 120 Table 4e. Anisotropic displacement parameters (Å² × 10³) for Form_B. The anisotropic displacement factor exponent takes the form: −2 pi² [ h² a*² U11 + . . . + 2 h k a* b* U12 ] U11 U22 U33 U23 U13 U12 Cl  71(1)  66(1)  86(1)    5(1)  −1(1) −13(1) O(33) 102(1) 107(2)  74(1)   12(1) −17(1) −43(1) N(6)  63(1)  68(1)  59(1)    6(1)    3(1)   15(1) C(1)  68(1) 106(2) 122(3) −12(2)   14(2)   17(2) C(2)  52(1)  86(2)  85(2)  −1(1)  −1(1)   12(1) C(3)  52(1)  64(1)  60(1)    5(1)    4(1)  −2(1) C(4)  62(1)  54(1)  59(1)    4(1)  −1(1)    1(1) C(5)  68(1)  58(1)  65(1)    5(1)    9(1)    9(1) C(6) 102(2) 100(2)  87(2)   23(2)   33(2)   14(2) C(7)  95(2) 118(2)  73(2) −21(2) −12(2)    0(2) C(31)  53(1)  58(1)  59(1)    2(1)   12(1)    4(1) C(32)  60(1)  63(1)  61(1)    0(1)    8(1)  −8(1) C(33)  64(1)  81(2)  58(1)  −3(1)    7(1) −14(1) C(34)  69(1)  71(1)  81(2) −11(1)   15(1) −16(1) C(35)  87(2)  58(1)  80(2)    1(1)   24(1)  −3(1) C(36)  72(1)  58(1)  67(1)    4(1)   13(1)    6(1) C(41)  96(2)  71(1)  73(2)   14(1)    5(1)   24(1)

Example 14: RAMAN Spectrum of Forms A and B

Form A and B were investigated using RAMAN spectroscopy. The RAMAN spectrometer used was a Bruker Raman FT 100. The RAMAN Microscope was a Renishaw 1000 System, 20× Obj. Long working distance, diode laser 785 nm. Raman spectroscopy was able to distinguish clearly between Forms A and B. Differences between the spectra of the two forms appear in the whole spectral range (3200-50 cm⁴), but the difference in the range between 800-200 cm-1 were most significant.

The results for Form A are shown in FIG. 3, the results for Form B in FIG. 6.

Furthermore the samples were investigated by RAMAN microscopy. The spectra of both forms were also distinguishable. Here, spectra were taken in the wavenumber range of 2000-100 cm⁻¹.

Example 16: Variable Temperature X-Ray Powder Diffraction Experiment

A variable temperature X-ray powder diffraction experiment was run thereby producing Form B from Form A. Form A converted to Form B from 40-50° C. during the experiment. The result is reversible with Form B changing over into Form A at lower temperature.

The foregoing description and examples have been set forth merely to illustrate the invention and are not intended to be limiting. Since modifications of the described embodiments incorporating the spirit and substance of the invention may occur to persons skilled in the art, the invention should be construed broadly to include all variations within the scope of the appended claims and equivalents thereof. 

1. A process for producing a (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form A, said process comprising: dissolving a (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form B in acetone, acetonitrile or isopropanol to form a solution; leaving the solution to crystallize and isolating crystals of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form A.
 2. The process of claim 1, wherein said (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of Form B is dissolved in acetonitrile, and further comprising the steps of: stirring the solution; removing insoluble residue by filtering and evaporating the acetonitrile leaving (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of Form A to crystallize.
 3. The process according to claim 1, wherein said (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form B is dissolved in isopropanol at temperatures above room temperature, and after complete dissolution no further heat is provided and further comprising: adding seed crystals of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form A and then cooling the mixture down to ≦15° C.
 4. The process of claim 3, wherein said (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form B is dissolved in isopropanol at a temperature above 65° C. but not exceeding 80° C.
 5. The process of claim 3, wherein said mixture is cooled down to ≦10° C.
 6. The process of claim 3, wherein said mixture is cooled down to ≦5° C.
 7. The process according to claim 1, further comprising redissolving the (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form A in a solvent selected from acetone, acetonitrile and isopropanol, then optionally filtering the solution to remove any insoluble residue and optionally reducing the amount of solvent by evaporation, then allowing the solution to crystallize.
 8. The process of claim 7, wherein said solvent is the same as that used to form the (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of crystalline Form A before the step of redissovling.
 9. The process of claim 7, wherein during the step of allowing the solution to crystallize, the temperature is maintained at ≦15° C.
 10. The process of claim 7, wherein during the step of allowing the solution to crystallize, the temperature is maintained at ≦10° C.
 11. The process of claim 7, wherein during the step of allowing the solution to crystallize, the temperature is maintained at ≦5° C.
 12. A crystalline Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride produced by the process of: dissolving (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of Form B in acetonitrile together with active carbon, heating the solution to the boiling point, removing the active carbon by filtering, stirring the solution at a temperature below 40° C., removing insoluble residue by filtering and removing part of the solvent, leaving (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of Form A to crystallize, redissolving the resulting crystals in acetonitrile, removing insoluble residue by filtering and removing part of the solvent, and leaving (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of Form A to crystallize.
 13. A pharmaceutical composition comprising, as an active ingredient, a crystalline Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride exhibiting at least X-ray lines (2-theta values) in a powder diffraction pattern when measured using Cu K_(α) radiation at 15.1±0.2, 16.0±0.2, 18.9±0.2, 20.4±0.2, 22.5±0.2, 27.3±0.2, 29.3±0.2 and 30.4±0.2, and at least one suitable additive or auxiliary substance.
 14. A pharmaceutical composition comprising, as an active ingredient, a crystalline Form A of (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride produced by the process of dissolving (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of Form B in acetonitrile together with active carbon, heating the solution to the boiling point, removing the active carbon by filtering, stirring the solution at a temperature below 40° C., removing insoluble residue by filtering and removing part of the solvent, leaving (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of Form A to crystallize, redissolving the resulting crystals in acetonitrile, removing insoluble residue by filtering and removing part of the solvent, and leaving (−)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride of Form A to crystallize, and at least one suitable additive or auxiliary substance. 